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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889369Generated: October 30, 2026

Triethylamine → ethyl 3-(1H-benzotriazol-1-yl)-2-cyclohexyl-3-oxopropanoate

https://huagongshe.com/reaction/889369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorocarbonyl-cyclohexyl-acetic acid ethyl esterHCID 86640284—
ReactantHCID 178418385HCID 178418385—
SolventDichloromethaneHCID 6344—
Productethyl 3-(1H-benzotriazol-1-yl)-2-cyclohexyl-3-oxopropanoateHCID 372228225%

Reaction Steps

A solution of 2-cyclohexyl-malonic acid monoethyl ester (2.9 g, 14 mmol; CAS Reg. No. 147596-63-2) in thionyl chloride (29 ml) was heated under reflux conditions for 2 h. The solvent was removed under reduced pressure to give chlorocarbonyl-cyclohexyl-acetic acid ethyl ester. 1,2,3-Benzotriazole (1.47 g, 12 mmol) was dissolved at ambient temperature under an argon atmosphere in CH2Cl2 (45 ml). Et3N (1.86 ml, 13 mmol) and a solution of chlorocarbonyl-cyclohexyl-acetic acid ethyl ester in CH2Cl2 (4 ml) was added. The reaction mixture was stirred at ambient temperature for 14 h, quenched with ice cold aqueous 2 N HCl and extracted two times with iPrOAc. The combined extracts were washed with ice water/1 N aqueous HCl solution, ice water/brine 1/1 and dried over Na2SO4. After filtration the solvent was removed under reduced pressure to give a yellow oil which was purified by column chromatography (silica gel, iPrOAc/heptane) to give the title compound (1.05 g, 3.3 mmol; 25%) as yellow oil. MS: m/e=316.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252826B2
Source datasetuspto-grants-2012_08
ORD IDord-4efb360494274c1b95bf8376478aa189
Source noteuspto-grants-2012_08